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临床试验/NCT04815876
NCT04815876已完成不适用

Randomized Trial Comparing Transperineal vs. Transrectal MRI-targeted Prostate Biopsy; Randomized Controlled Trial Assessing Transperineal Prostate Biopsy to Reduce Infection Complications

Weill Medical College of Cornell University17 个研究点 分布在 1 个国家目标入组 1,040 人开始时间: 2021年6月24日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
1,040
试验地点
17
主要终点
Change in infection adverse events, as measured on TRUS-BxQ

研究概览

简要总结

Approximately one million transrectal prostate biopsies are performed annually in the U.S., and the risk of post- biopsy infection is increasing due to greater antibiotic resistance of rectal flora. Preliminary data demonstrates that a transperineal MRI-targeted biopsy approach under local anesthesia compared to the standard practice transrectal MRI-targeted prostate biopsy has a much lower risk of infection, comparable pain/discomfort and may improve detection of prostate cancer.

This randomized controlled trial will be the first prospective study to evaluate in-office transperineal MRI targeted prostate biopsy.

The investigators hypothesize that a transperineal MRI-targeted biopsy approach under local anesthesia compared to the standard practice transrectal MRI-targeted prostate biopsy has a much lower risk of infection, comparable pain/discomfort and may improve detection of prostate cancer.

详细描述

Prostate cancer is the most commonly diagnosed malignancy in U.S. men. There are approximately 1 million prostate biopsy performed annually in the U.S. Almost all biopsies are performed as an office based procedure in under 15 minutes. The precision of biopsy has improved over the last decade with the introduction of MRI guidance/targeting of suspicious lesions within the prostate.

However, significant limitations remain with this approach, including a significantly increasing risk of post-biopsy infection. This arises because more than 97% of all prostate biopsy are performed via a transrectal approach that introduces rectal bacteria with each pass of the biopsy needle into the sterile urinary tract. The current risk of post-transrectal biopsy infection, even with antimicrobial prophylaxis, is high at approximately 7% overall with 3% (30,000 men) requiring hospitalization annually.

Transperineal biopsy is an alternate approach that eliminates the direct introduction of bacteria from the rectum to the prostate. This approach, which is performed without antimicrobial prophylaxis, instead passes the biopsy needle through the perineal skin and pelvic floor.

Transperineal biopsy has not been widely adopted for several reasons. Historically, it has been considered too painful for patients in the clinic and thus was traditionally performed under general anesthesia. The added time, inconvenience and cost has limited its national adoptance. Second, when transrectal biopsy was initially adopted over 40 years ago, antibiotic resistance of rectal flora was not a challenge.

Beyond the potential for in-office transperineal biopsy to significantly reduce or eliminate biopsy infections, transperineal biopsy may also improve cancer detection: studies of transperineal biopsy (performed under general anesthesia) demonstrate higher detection rates for prostate cancer, particularly for anterior zone tumors, compared to transrectal biopsy. This is notable, as anterior tumors are difficult to sample with transrectal. Anterior tumors are also twice as likely to occur in African American men. In fact, our research demonstrates that some of the outcomes disparities in African American men may stem from an underdiagnosis of anterior prostate cancers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Outcomes Assessor)

盲法说明

Radiologists assessing MRI results are blinded to treatment assignment. Pathologists assessing biopsy results are blinded to treatment assignment.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Active surveillance cohort: History of Grade Group 1 prostate cancer, first diagnosed ≤24 months prior to date of planned confirmatory biopsy and diagnostic biopsy was preceded by a multiparametric MRI of the prostate
  • Prior negative cohort: Clinical concern for the presence of prostate cancer as determined by the treating urologist and prior negative prostate biopsy performed ≤36 months prior to date of planned biopsy
  • Willingness to sign informed consent and adhere to the study protocol

排除标准

  • Acute prostatitis within the last 6 months
  • Current non-urologic bacterial infection requiring active treatment with antibiotics
  • Unfit to undergo prostate biopsy under local anesthesia
  • Prior definitive therapy for prostate cancer, such as radiation therapy or partial gland ablation
  • Contraindication to prostate MRI (claustrophobia, pacemaker, chronic kidney disease)

研究组 & 干预措施

Transrectal

Active Comparator

Patients will receive a transrectal MRI-guided prostate biopsy.

干预措施: Transrectal MRI-guided prostate biopsy (Procedure)

Transrectal

Active Comparator

Patients will receive a transrectal MRI-guided prostate biopsy.

干预措施: Antibiotic (prophylaxis) (Drug)

Transperineal

Active Comparator

Patients will receive a transperineal MRI-guided prostate biopsy.

干预措施: Transperineal MRI-guided prostate biopsy (Procedure)

结局指标

主要结局

Change in infection adverse events, as measured on TRUS-BxQ

时间窗: At initiation of biopsy, immediately following biopsy, 7 days post-biopsy

TRUS-BxQ is a validated biopsy questionnaire that measures adverse events that have occurred due to infection. Patient questionnaire consists of Yes/No questions about infection complications and duration of infection.

Number of Participants With Infection/Adverse Events, as Measured on the TRUS-Bx Questionnaire

时间窗: up to 7- 10 days post-biopsy

TRUS-BxQ is a validated biopsy questionnaire that measures adverse events that have occurred due to infection. Patient questionnaire consists of Yes/No questions about infection complications and duration of infection.

次要结局

  • Change in patient-reported pain and discomfort, as measured on a 0-10 Likert scale(Immediately following biopsy, 7 days post-biopsy)
  • Change in patient-reported anxiety, as measured on a 0-10 Likert scale(Immediately following biopsy, 7 days post-biopsy)
  • Detection of clinically significant disease as measured by Gleason Grade Group ≥ 2(7 days post-biopsy)
  • Change in adverse events, as measured on TRUS-BxQ(At initiation of biopsy, immediately following biopsy, 7 days post-biopsy)
  • Change in Patient-reported Pain and Discomfort, as Measured on a 0-10 Likert Scale(Immediately following biopsy, 7 days post-biopsy)
  • Change in Patient-reported Anxiety, as Measured on a 0-10 Likert Scale(Immediately following biopsy)
  • Number of Participants With Detection of Clinically Significant Disease as Measured by Gleason Grade Group ≥ 2(7 days post-biopsy)
  • Number of Adverse Events, as Measured on TRUS-BxQ(up to 7-10 days post-biopsy)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (17)

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